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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587801Generated: October 30, 2026

CID 71433830 → N-((1R,2S)-1-benzyl-7-bromo-1,2,3,4-tetrahydronaphthalen-2-yl)propionamide

https://huagongshe.com/reaction/587801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCID 71433830HCID 71433830—
ReactantN-(1-benzyl-7-bromo-3,4-dihydronaphthalen-2-yl)propionamideHCID 86707883—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178478078HCID 178478078—
SolventEthanolHCID 702—
ProductN-((1R,2S)-1-benzyl-7-bromo-1,2,3,4-tetrahydronaphthalen-2-yl)propionamideHCID 7270716668%

Reaction Conditions

Temperature50 °C

Reaction Steps

Chlorocyclooctadiene rhodium(I) dimer (0.217 g, 0.881 mmol of Rh), Josiphos SL-J216-2 (0.595 g, 0.926 mmol), and N-(1-benzyl-7-bromo-3,4-dihydronaphthalen-2-yl)propionamide (10.88 g, 29.4 mmol) were combined in a metal reactor, and the vessel was inerted with argon. Degassed ethanol (163 ml) was added, and the mixture was agitated under argon for 30 min at 50° C. The vessel was pressurized with 60 psig of hydrogen and agitated at 55° C. for 14.5 hrs. HPLC analysis indicated 89.4% conversion and 93.8% ee. The mixture was concentrated, and the resulting solid was crystallized from MeOH to yield 7.41 g (yield: 68%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227901B2
Source datasetuspto-grants-2016_01
ORD IDord-48e0a33ec1524d12ba330d599da8f15b
Source noteuspto-grants-2016_01